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Teprotumumab

Alternative Names: teprotumumab, tepezza, teprotumumab-trbw, RV-001, RV001, RV 001, Onilcamotide
Latest Update: 2024-11-05
Latest Update Note: Clinical Trial Update

Product Description

Teprotumumab-trbw injection is used to treat thyroid eye disease (TED; Graves' eye disease; a disorder in which the immune system causes inflammation and swelling behind the eye). Teprotumumab-trbw is in a class of medications called monoclonal antibodies. It works by blocking the action of a certain protein in the body that causes inflammation in the eye. (Sourced from: https://medlineplus.gov/druginfo/meds/a620025.html)

Mechanisms of Action: IGF Antagonist

Novel Mechanism: No

Modality: Antibody

Route of Administration: Intravenous

FDA Designation: Fast Track - Prostate Cancer *

Approval Status: Approved

Approved Countries: Greece | United States

Approved Indications: None

Known Adverse Events: None

Company: Amgen
Company Location: THOUSAND OAKS CA 91320
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Teprotumumab

Countries in Clinic: Argentina, Australia, Canada, France, Germany, Italy, Japan, Poland, South Korea, Spain, Taiwan, United Kingdom, United States

Active Clinical Trial Count: 8

Highest Development Phases

Phase 3: Graves Disease|Graves Ophthalmopathy|Thyroid Eye Disease

Phase 2: Prostate Cancer

Phase 1: Neuromyelitis Optica

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

jRCT2031240294

P3

Recruiting

Thyroid Eye Disease

2026-07-31

jRCT2031220730

P3

Recruiting

Thyroid Eye Disease

2026-06-30

TEPEZZA (teprotumumab-trbw) Post-Marketing Requirement

P3

Active, not recruiting

Thyroid Eye Disease

2026-01-24

HZNP-TEP-305

P3

Recruiting

Graves Disease|Thyroid Eye Disease|Graves Ophthalmopathy

2025-10-15

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